Search Results - "McNaull, Melissa N."

Characterization of the severe phenotype of pyruvate kinase deficiency by Al‐Samkari, Hanny, Beers, Eduard J., Morton, D. Holmes, Barcellini, Wilma, Eber, Stefan W., Glader, Bertil, Yaish, Hassan M., Chonat, Satheesh, Kuo, Kevin H. M., Kollmar, Nina, Despotovic, Jenny M., Pospíšilová, Dagmar, Knoll, Christine M., Kwiatkowski, Janet L., Pastore, Yves D., Thompson, Alexis A., Wlodarski, Marcin W., Ravindranath, Yaddanapudi, Rothman, Jennifer A., Wang, Heng, Holzhauer, Susanne, Breakey, Vicky R., Verhovsek, Madeleine M., Kunz, Joachim, Sheth, Sujit, Sharma, Mukta, Rose, Melissa J., Bradeen, Heather A., McNaull, Melissa N., Addonizio, Kathryn, Al‐Sayegh, Hasan, London, Wendy B., Grace, Rachael F.

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Genotype-Phenotype Correlation and Molecular Heterogeneity in Pyruvate Kinase Deficiency: Data from the PKD Natural History Study by Bianchi, Paola, Fermo, Elisa, Lezon-Geyda, Kimberly, Gallagher, Patrick G., van Wijk, Richard, Van Beers, Eduard J., Yaish, Hassan M., Kwiatkowski, Janet L., Newburger, Peter E., Ravindranath, Yaddanapudi, Andres, Oliver, Barcellini, Wilma, Morton, D. Holmes, Glader, Bertil, Eber, Stefan W., Chonat, Satheesh, Kollmar, Nina, Despotovic, Jenny M., Knoll, Christine M., Kuo, Kevin H.M., Pospisilova, Dagmar, Pastore, Yves D., Thompson, Alexis A, Wang, Winfred, Wlodarski, Marcin W., Rothman, Jennifer A., Wang, Heng, Holzhauer, Suzanne, Breakey, Vicky R., Kunz, Joachim B., Sheth, Sujit, Sharma, Mukta, Rose, Melissa J., Bradeen, Heather A., McNaull, Melissa N., Ooyama, Gabrielle P., Neu, Nolan, Al-Sayegh, Hasan, London, Wendy B., Grace, Rachael F.

“…Background: Pyruvate kinase (PK) deficiency is the most common enzyme defect of the glycolytic pathway causing hereditary non-spherocytic hemolytic anemia. PK…”
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